Package 0615-8141-39

Brand: citalopram

Generic: citalopram hydrobromide
NDC Package

Package Facts

Identity

Package NDC 0615-8141-39
Digits Only 0615814139
Product NDC 0615-8141
Product ID 0615-8141_aec16083-ac47-4a94-83ca-412b543f477e
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8141-39)

Marketing

Marketing Status
Marketed Since 2018-01-05
Brand citalopram
Generic citalopram hydrobromide
Sample Package No

Linked Drug Pages (1)

Citalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "aec16083-ac47-4a94-83ca-412b543f477e", "openfda": {"unii": ["I1E9D14F36"], "rxcui": ["200371", "283672", "309314"], "spl_set_id": ["fd761647-e16b-45b3-a4bc-364de0ed7015"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8141-39)", "package_ndc": "0615-8141-39", "marketing_start_date": "20180105"}], "brand_name": "Citalopram", "product_id": "0615-8141_aec16083-ac47-4a94-83ca-412b543f477e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0615-8141", "generic_name": "Citalopram Hydrobromide", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Citalopram", "active_ingredients": [{"name": "CITALOPRAM HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077031", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}